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Research 61–90 of 502
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Disease causing homozygous variants in the human hairless gene
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Serum sickness–like reaction in children: A retrospective review
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Measuring the impact on quality of life of infants with atopic dermatitis in a dedicated clinic
- Treatment of frontal fibrosing alopecia: literature review 2020-2025
- The Rotterdam Study: 2016 objectives and design update
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Alopecia areata
- An Update of Congenital Adrenal Hyperplasia
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Dermatoses of Pregnancy - Clues to Diagnosis, Fetal Risk and Therapy
- Dermatologic manifestations of endocrine disorders
- Learning from nudity: lessons from the nude phenotype
- Pathways to inflammation: acne pathophysiology
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Prediction of male-pattern baldness from genotypes
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Skin disease in pregnancy
- Dermatoses of pregnancy